Canonical Allele Identifier: CA392044329

Gene: CDAN1

Linked Data

• gnomAD v4: 15-42731214-C-G
• MyVariant Identifiers: chr15:g.43023412C>G (hg19) ; chr15:g.42731214C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731214C>G , CM000677.2:g.42731214C>G	GRCh38
NC_000015.9:g.43023412C>G , CM000677.1:g.43023412C>G	GRCh37
NC_000015.8:g.40810704C>G	NCBI36
NG_012491.1:g.11006G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1857G>C MANE Select	ENSP00000348564.3:p.Trp619Cys
ENST00000643434.1:c.*1035G>C	ENSP00000494699.1:n.*1035G>C
ENST00000356231.3:c.1857G>C	ENSP00000348564.3:p.Trp619Cys
NM_138477.2:c.1857G>C	NP_612486.2:p.Trp619Cys
XM_005254176.3:c.1860G>C	XP_005254233.1:p.Trp620Cys
XM_011521270.1:c.1884G>C	XP_011519572.1:p.Trp628Cys
XM_011521271.1:c.1881G>C	XP_011519573.1:p.Trp627Cys
XM_011521272.1:c.1884G>C	XP_011519574.1:p.Trp628Cys
XM_011521273.1:c.1884G>C	XP_011519575.1:p.Trp628Cys
XM_011521274.1:c.849G>C	XP_011519576.1:p.Trp283Cys
XM_011521275.1:c.1101G>C	XP_011519577.1:p.Trp367Cys
XR_931757.1:n.1895G>C
NM_138477.4:c.1857G>C MANE Select	NP_612486.2:p.Trp619Cys
XM_005254176.5:c.1860G>C	XP_005254233.1:p.Trp620Cys
XM_011521270.2:c.1884G>C	XP_011519572.1:p.Trp628Cys
XM_011521271.2:c.1881G>C	XP_011519573.1:p.Trp627Cys
XM_011521274.2:c.849G>C	XP_011519576.1:p.Trp283Cys
XR_001751104.1:n.1914G>C
XR_001751105.1:n.1914G>C
XR_931757.2:n.1915G>C